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101.
Akie Uehara Tomonobu Senjyu Toshiaki Kaneko Atsushi Yona Endusa Billy Muhando Naomitsu Urasaki Chul‐Hwan Kim 《风能》2010,13(7):671-684
Nowadays, a wind turbine generator (WTG) is required to provide control capabilities as the output power of WTG fluctuates. Under this scenario, this paper proposes an output power control method of a wind farm (WF) connected to a small power system using pitch angle control. In this control approach, the WF output power control is achieved by two control levels: central and local. In the central control, the WF output power command is determined by considering the frequency deviations and wind speeds using a fuzzy function. Then, the local output power commands for each of the WTGs are based on the proposed dispatch control. In the proposed dispatch control, the output commands of each WTG are determined by considering wind conditions for each of the WTGs. The simulation results by using an actual detailed model for the wind power system show the effectiveness of the proposed method. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
102.
Grain growth in a high-purity ZnO and for the same ZnO with Bi2 O3 additions from 0.5 to 4 wt% was studied for sintering from 900° to 1400°C in air. The results are discussed and compared with previous studies in terms of the phenomenological kinetic grain growth expression: G n — G n 0 = K 0 t exp(— Q/RT ). For the pure ZnO, the grain growth exponent or n value was observed to be 3 while the apparent activation energy was 224 ± 16 kJ/mol. These parameters substantiate the Gupta and Coble conclusion of a Zn2+ lattice diffusion mechanism. Additions of Bi2 O3 to promote liquidphase sintering increased the ZnO grain size and the grain growth exponent to about 5, but reduced the apparent activation energy to about 150 kJ/mol, independent of Bi2 O3 content. The preexponential term K 0 was also independent of Bi2 O3 content. It is concluded that the grain growth of ZnO in liquid-phase-sintered ZnO-Bi2 O3 ceramics is controlled by the phase boundary reaction of the solid ZnO grains and the Bi2 O3 -rich liquid phase. 相似文献
103.
W.-C. Xu K. Takahashi Y. Matsuo Y. Hattori M. Kumagai S. Ishiyama K. Kaneko S. Iijima 《International Journal of Hydrogen Energy》2007
Hydrogen storage capacity of various carbon materials, including activated carbon (AC), single-walled carbon nanohorn, single-walled carbon nanotubes, and graphitic carbon nanofibers, was investigated at 303 and 77 K, respectively. The results showed that hydrogen storage capacity of carbon materials was less than 1 wt% at 303 K, and a super activated carbon, Maxsorb, had the highest capacity (0.67 wt%). By lowering adsorption temperature to 77 K, hydrogen storage capacity of carbon materials increased significantly and Maxsorb could store a large amount of hydrogen (5.7 wt%) at a relatively low pressure of 3 MPa. Hydrogen storage capacity of carbon materials was proportional to their specific surface area and the volume of micropores, and the narrow micropores was preferred to adsorption of hydrogen, indicating that all carbon materials adsorbed hydrogen gas through physical adsorption on the surface. 相似文献
104.
Xiande Shen Yoshikazu Kitajyo Qian Duan Atsushi Narumi Harumi Kaga Noriaki Kaneko Toshifumi Satoh Toyoji Kakuchi 《Polymer Bulletin》2006,56(2-3):137-143
Summary The reaction of the carboxymethyl cellulose sodium salt (Na-CMC) (degrees of substitution (DS) = 1.2) with N-hydroxysuccinimide (Su-OH) in the presence of 1-hydroxybenzotriazole and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)
was carried out in water to obtain the Su-OH ester of carboxymethyl cellulose, Su-CMC, with the DS values of 0.19 – 1.04.
N-Allylcarbamoylmethyl cellulose (Allyl-CMC), which was prepared from the reaction of Su-CMC with an excess amount of allylamine,
was crosslinked by UV-irradiation. In addition, the photocrosslinked Allyl-CMC film was swollen with water to form a hydrogel
having a relatively high water-swelling property, e.g., the degree of swelling (ds) was ca. 360% for Allyl-CMC with the DS
of 0.93. 相似文献
105.
106.
Yunosuke Abe Toshiki Aoki Hongge Jia Shingo Hadano Takeshi Namikoshi Yuriko Kakihana Lijia Liu Yu Zang Masahiro Teraguchi Takashi Kaneko 《Polymer》2012,53(11):2129-2133
A soluble and stable one-handed helical conjugated polymer without the coexistence of any other chiral moieties was successfully synthesized by asymmetric-induced polymerization of a chiral monomer having two hydroxyl groups followed by desubstitution of the chiral groups in a solid membrane state. The reason for the success was the polymer reaction was carried out in the membrane state. This is an alternative method to obtain such a unique chiral polymer which was obtained only by the helix-sense-selective polymerization (HSSP) we reported before. In addition the efficiency of the chiral induction was higher than that of the HSSP. It is interesting that the “Membrane state” acted like as if a protecting group. 相似文献
107.
Rosiah Rohani Tetsuya Yamaki Hiroshi Koshikawa Shin Hasegawa Yasunari Maekawa Christina Trautmann 《Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms》2009,267(3):554-557
We investigated how pretreatment and high-LET beam irradiation affected the ion-track dissolution rate in poly(vinylidene fluoride) (PVDF) films by SEM observations and conductometric analysis in order to develop the preparation methodology of nano-sized ion-track membranes. PVDF thin films irradiated with four types of ion beams were exposed to a 9 mol/dm3 KOH aqueous solution after their storage in air at 120 °C. This heating treatment was found to enhance the etch rate in the latent track, both in the inner core and outer halo regions, without changing that in the bulk, probably due to the formation of parasitic oxidation products facilitating the introduction of the etching agent to improve the etchability. Additionally, the irradiation of heavier higher-LET ions, causing each track to more activated sites (like radicals), was preferable for achieving effective etching. 相似文献
108.
Tetsuya Muramoto 《Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms》2009,267(18):3232-3234
Temperature dependence of sputtering yield is studied through molecular dynamics (MD) simulation that is performed for Ag sputtered by 12.6 keV Ar impacting at normal incidence. The target temperature is considered from 300 to 1235 K. It is found that the target temperature has little effect on the monomer yield because it comes from the energetic collision cascade. On the other hand, the sputtered cluster yield increases with the target temperature. It seems that the sputtered cluster is produced due to the thermal spike near the surface and the thermal spike is strongly influenced by the target temperature. 相似文献
109.
The purpose of the present investigation was to test whether permanent skeletal muscle cells (rat L6 cells) could serve as
an in vitro model for α-tocopherol (αTocH) biodiscrimination studies. L6 cells were incubated in the presence of high density lipoprotein
(HDL), low density lipoprotein (LDL), and very low density lipoprotein (VLDL) labeled in the lipid moiety with either all-rac-or RRR-[14C]αTocH. These incubations were performed either in the absence or in the presence of exogenously added bovine lipoprotein
lipase (LPL) since skeletal muscle is one of the major expression sites of LPL in vivo. Time-dependent uptake studies (up to 24 h) in the absence of LPL have shown that equipotent doses of all-rac- and RRR-[14C]αTocH (1.36∶1) led to almost identical accumulation of the tracer, independent of the lipoprotein class used as αTocH carrier.
With regard to αTocH donor capacity, it appeared that HDL is the most potent αTocH donor, followed by LDL and VLDL. In the
presence of LPL, all-rac- and RRR-[14C]αTocH uptake was significantly enhanced (between two- and tenfold). Biodiscrimination studies using chiral high-performance
liquid chromatographic analysis with radiometric detection of the corresponding methyl ether derivatives on a Chiralcel OD
column have demonstrated that the 2S-and 2R-isomers of αTocH were taken up in a 1∶1 ratio by L6 cells independent of the absence or presence of LPL. In addition, we
have not observed biodiscrimination between the four 2R-isomers, i.e., there was no preferential accumulation of the RRR-isomer. These data suggest that L6 cells do not discriminate between different αTocH isomers and that the addition of endogenous
LPL significantly enhances the uptake of RRR- and all-rac-αTocH. 相似文献
110.
Tetsuya Araki Yasuyuki Sagara Kamaruddin Abdullah Armansyah H. Tambunan 《Drying Technology》2001,19(2):297-312
The samples of sliced and mashed apples were freeze-dried by controlling their surface temperatures over the usual pressure range of commercial operations. The surface of sliced samples could not be maintained at above 10°C in order to prevent the frozen layer from melting, while that of mashed samples was allowed to heat up to 70°C.
Thermal conductivities and permeabilities were determined by applying the uniformly-retreating-ice front model to the dried layer of the samples undergoing freeze-drying. The values of permeability for the mashed samples were found to depend on the ice-crystallization time during freezing. The results indicated that the drying rate of sliced samples was limited by the transfer rate of water vapor flowing through the dried layer. A cellular structural model is proposed for predicting the permeability of the dried layer, based on the resistance of the cell membrane to molecular transfer of water vapor. 相似文献
Thermal conductivities and permeabilities were determined by applying the uniformly-retreating-ice front model to the dried layer of the samples undergoing freeze-drying. The values of permeability for the mashed samples were found to depend on the ice-crystallization time during freezing. The results indicated that the drying rate of sliced samples was limited by the transfer rate of water vapor flowing through the dried layer. A cellular structural model is proposed for predicting the permeability of the dried layer, based on the resistance of the cell membrane to molecular transfer of water vapor. 相似文献